Silica-Supported Gold Nanocatalyst for CO Oxidation

Ziyauddin S. Qureshi, E. Jaseer
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引用次数: 4

Abstract

Even though gold is inert in its bulk practice, greatly disseminated gold nanoparticles (Au NPs) with dimensions less than 5 nm have been found to be active for a number of oxygen transfer reactions, particularly for low-temperature CO oxidation. The catalytic activity not only be subject to the particle size of Au but also on the nature of the support and the synthesis method of the catalyst. These factors are frequently inter-related such that their separate contributions cannot be easily unrav-eled. Also, the activity of a supported Au catalyst is ruled by a complex combination of contributions of the particle morphology, metal dispersion, and electronic properties of the gold. Higher catalytic activity is being observed for Au NPs supported on reducible metal oxides such as TiO 2 , Co 3 O 4 , CeO 2 , and Fe 2 O 3 . However, silica is an inert, inexpensive, and convenient support that can be shaped into a host of attractive and varied morphologies. In this chapter, the study of CO oxidation catalyzed by mono- and bimetallic Au NPs over various silica supports is discussed in detail.
二氧化硅载金纳米CO氧化催化剂
尽管金在体积上是惰性的,但尺寸小于5nm的大面积分布的金纳米颗粒(Au NPs)已被发现在许多氧转移反应中是活跃的,特别是在低温CO氧化中。催化剂的催化活性不仅与Au的粒径大小有关,还与载体的性质和催化剂的合成方法有关。这些因素往往是相互关联的,因此它们各自的贡献不能轻易地加以解释。此外,负载型金催化剂的活性是由金的粒子形态、金属分散和电子性质的复杂组合决定的。在还原性金属氧化物如tio2、co2o3、ceo2和fe2o3上负载的Au NPs具有较高的催化活性。然而,二氧化硅是一种惰性的,廉价的,方便的支持,可以塑造成许多有吸引力的和不同的形态。在本章中,详细讨论了单金属和双金属金纳米粒子在不同二氧化硅载体上催化CO氧化的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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